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Phenotypes Associated with This Genotype
Genotype
MGI:6163707
Allelic
Composition		 Foxg1tm1(cre)Skm/?
Gt(ROSA)26Sorem1(ptxA)Btar/?
Genetic
Background		 involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxg1tm1(cre)Skm mutation (2 available); any Foxg1 mutation (30 available)
Gt(ROSA)26Sorem1(ptxA)Btar mutation (0 available); any Gt(ROSA)26Sor mutation (1027 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
hearing/vestibular/ear
abnormal cochlear hair cell stereociliary bundle morphology ( J:236519 )
• at birth the apical hair cells show severe bundle misorientation

mortality/aging

nervous system
abnormal cochlear hair cell stereociliary bundle morphology ( J:236519 )
• at birth the apical hair cells show severe bundle misorientation

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
03/18/2025
MGI 6.24 		The Jackson Laboratory